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Csv Engineer Jobs (NOW HIRING)

Eliquent Life Sciences, Inc

CSV Engineer

Mount Horeb, WI · On-site

$120K - $135K/yr

The CSV Engineer will author validation deliverables--including protocols, reports, and SOPs--ensuring compliance with FDA, EMA, and global regulatory expectations. Key Responsibilities: * Develop ...

Katalyst CRO

CSV Engineer

Redwood City, CA · On-site

... CSV Engineer • Ensuring compliance with validation and regulatory standards Qualifications : Required : • Strong CSV (Computer System Validation) experience • Hands-on experience with Veeva ...

Nanda Technologies

CSV Engineer

Costa Mesa, CA · On-site

$55 - $60/hr

CSV Engineer Costa Mesa, CA or Seattle, WA(On-site) Visa: USC, GC & H4 EAD Key Responsibilities: * Develop and maintain Design Specifications (DS) for computerized and automated systems. * Author and ...

Workforce Genetics

CSV Engineer

Baltimore, MD

CSV Engineer (6mo. Contract-to-Hire) Location: Baltimore, MD Company Join a premier global Contract Development and Manufacturing Organization (CDMO) that is rapidly expanding its state-of-the-art ...

PM Group

CSV Engineer I

Indianapolis, IN

$68K - $88K/yr

Overview The CSV Engineer I position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a site near Indianapolis, IN . Outsourced Technical ...

PM Group

CSV Engineer III

Indianapolis, IN · On-site

$68K - $88K/yr

Overview The CSV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a site near Indianapolis, IN . Outsourced Technical ...

PM Group

CSV Engineer III

Indianapolis, IN

$68K - $88K/yr

Overview The CSV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a site near Indianapolis, IN . Outsourced Technical ...

PM Group

CSV Engineer I

Indianapolis, IN · On-site

$68K - $88K/yr

Overview The CSV Engineer I position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a site near Indianapolis, IN . Outsourced Technical ...

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Csv Engineer information

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$36K

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How much do csv engineer jobs pay per year?

As of Aug 17, 2026, the average yearly pay for csv engineer in the United States is $99,411.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What is the salary of CSV engineer?

The salary of a CSV engineer typically ranges from $70,000 to $120,000 annually, depending on experience, location, and industry. Skilled professionals with expertise in data processing, scripting, and database management tend to earn higher salaries. Certifications in data engineering or related tools can also influence compensation.

How much do CSV engineers make?

CSV engineers typically earn between $70,000 and $120,000 annually, depending on experience, location, and industry. Skilled professionals with expertise in data processing, scripting, and database management tend to command higher salaries.

What is a CSV engineer?

A CSV (Computer System Validation) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, comply with regulatory requirements. They develop validation protocols, perform testing, document results, and ensure adherence to industry standards like FDA 21 CFR Part 11 and GAMP 5. Their goal is to confirm that software and hardware systems function correctly, maintain data integrity, and meet compliance requirements.

What does a CSV engineer do?

A CSV engineer specializes in designing, developing, and maintaining systems that process and manage data stored in CSV (comma-separated values) format. They often work with data pipelines, scripting languages like Python or SQL, and data validation tools to ensure accurate data handling and integration across applications.

What are the common challenges faced by a CSV engineer in the pharmaceutical or medical device industry?

CSV Engineers in the pharmaceutical or medical device industry often face the challenge of keeping up with evolving regulatory requirements and ensuring all computerized systems remain compliant throughout their lifecycle. Managing comprehensive documentation, coordinating with multiple departments, and troubleshooting complex system changes can add to the workload. Successful CSV Engineers are proactive about staying informed of regulatory updates, are highly organized, and collaborate closely with Quality Assurance, IT, and operations teams. This dynamic environment offers the opportunity to learn continuously, develop expertise in validation best practices, and advance into leadership or specialized quality roles.

What are the key skills and qualifications needed to thrive as a CSV engineer?

To thrive as a CSV Engineer (Computer System Validation Engineer), you need a solid understanding of validation principles, regulatory compliance (such as FDA 21 CFR Part 11), and a relevant degree in life sciences, engineering, or information technology. Familiarity with validation lifecycle documentation, risk assessment tools, and industry-standard systems like SAP, LIMS, and TrackWise is highly valued, as are certifications such as GAMP or Six Sigma. Strong attention to detail, analytical thinking, and excellent communication skills help CSV Engineers collaborate efficiently with cross-functional teams and ensure thorough documentation. These skills are crucial to guarantee that computerized systems in regulated industries meet compliance requirements, supporting product quality and patient safety.

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Csv Engineer jobs near you
Infographic showing various Csv Engineer job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $99,411 per year, or $47.8 per hour.

CSV Engineer

Katalyst Healthcares and Lifesciences

Cincinnati, OH • On-site

Other

Posted 3 days ago

New

Job description

Job Description:
  • The CSV Engineer is responsible for ensuring that GxP computerized systems at the client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5).
  • This role directly supports gene therapy manufacturing operations by leading validation activities for key systems, including Veeva QMS, BMRAM, analytical lab instruments, and the Metasys Client.
  • By maintaining data integrity and system compliance, the CSV Engineer plays a critical part in ensuring product quality, patient safety, and regulatory inspection readiness.
Roles & Responsibilities:
  • uthor, review, and execute validation deliverables for GxP computerized systems, including Validation Plans, Requirements Specifications (URS/FS/DS), IQ/OQ/PQ protocols, Trace Matrices, and Validation Summary Reports.
  • Support computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information management), analytical lab instruments (e.g., HPLC, UHPLC, PCR instruments, plate readers etc.), ERP System (NetSuite).
  • Perform risk assessments to determine validation approach and ensure appropriate testing of system functionality, data integrity, and audit trail review.
  • Manage system change control, deviations, and CAPAs related to validated systems, ensuring compliance with Forge's quality system.
  • Collaborate with IT, QA, Lab Operations, and Facilities teams to support system upgrades, patches, and periodic reviews while maintaining a validated state.
Requirements:
  • Bachelor's degree in Computer Science, Engineering, Life Sciences, or related field (or equivalent experience).
  • 5-7+ years of experience in Computer System Validation (CSV) within a GxP regulated environment (pharmaceutical, biotech, or medical device).
  • Working knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles (ALCOA+).
  • Experience validating at least one of the following: Veeva Vault QMS, BMRAM, laboratory instrumentation (e.g., Waters, Agilent, Chromeleon, Softmax or similar), or a building management system (Client) like Metasys.
  • Strong technical writing skills and ability to execute protocols with minimal supervision.
  • Nice to have: BMRAM and analytical lab instruments experience.

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